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rs730880855

From SNPedia

Orientationminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs730880855(A;G)
Make rs730880855(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23431425
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880855
ebirs730880855
HLIrs730880855
Exacrs730880855
Varsomers730880855
Maprs730880855
PheGenIrs730880855
hapmaprs730880855
1000 genomesrs730880855
hgdprs730880855
ensemblrs730880855
gopubmedrs730880855
geneviewrs730880855
scholarrs730880855
googlers730880855
pharmgkbrs730880855
gwascentralrs730880855
openSNPrs730880855
23andMers730880855
23andMe allrs730880855
SNP Nexus

SNPshotrs730880855
SNPdbers730880855
MSV3drs730880855
GWAS Ctlgrs730880855
Max Magnitude0
ClinVar
Risk rs730880855(G;G)
Alt rs730880855(G;G)
Reference rs730880855(A;A)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not specified
Variation info
Gene MYH7
CLNDBN Primary familial hypertrophic cardiomyopathy not specified
Reversed 1
HGVS NC_000014.8:g.23900634T>C
CLNSRC
CLNACC RCV000208372.1, RCV000223688.1,